Literature DB >> 10493481

Detrimental effects of standard medical therapy in congenital diaphragmatic hernia.

D W Kays1, M R Langham, D J Ledbetter, J L Talbert.   

Abstract

OBJECTIVE: To evaluate the impact of a nonstandard ventilation strategy on survival in congenital diaphragmatic hernia (CDH).
BACKGROUND: Despite recent advances, including nitric oxide, CDH remains an unsolved problem with a mortality rate of 35% to 50%. Hyperventilation and alkalization remain common therapies.
METHODS: In 1992, the authors prospectively abandoned hyperventilation and alkalization. Patients are lightly sedated and ventilated with the lowest pressure providing adequate chest movement, and the rate is set to patient comfort. Nitric oxide and extracorporeal membrane oxygenation (ECMO) are reserved for life-threatening instability. Surgical repair is delayed 1 to 5 days. Sixty consecutive patients are compared with 29 previous patients treated with hyperventilation and alkalization, 13 before and 16 after the availability of ECMO.
RESULTS: Overall, 47 of 60 patients (78%) in study era 3 survived compared with 2 of 13 (15%) in the hyperventilation era and 7 of 16 (44%) in the hyperventilation/ECMO era (p < 0.0001). The disease severity and the incidence of associated anomalies did not differ between groups. To compare management strategies, patients who had treatment withheld because of lethal associated conditions were then removed from analysis. Peak inspiratory pressure and arterial pH were lower (p < 0.0001) and Paco2 was higher (p < 0.05) in era 3 than in the previous eras. The rate of pneumothorax (1.9%) decreased (p < 0.0001). In era 3, survival was 47 of 53 (89%) treated patients, and 23 of 25 inborn patients with isolated CDH survived (92%).
CONCLUSIONS: Nonstandard ventilatory support of patients with CDH has led to significantly improved survival rates. This study sets a survival benchmark and strongly suggests the negative effects of hyperventilation and alkalization.

Entities:  

Mesh:

Year:  1999        PMID: 10493481      PMCID: PMC1420879          DOI: 10.1097/00000658-199909000-00007

Source DB:  PubMed          Journal:  Ann Surg        ISSN: 0003-4932            Impact factor:   12.969


  41 in total

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5.  Congenital diaphragmatic hernia. New concept in management.

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Authors:  J T Wung; L S James; E Kilchevsky; E James
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8.  Correction of congenital diaphragmatic hernia in utero IX: fetuses with poor prognosis (liver herniation and low lung-to-head ratio) can be saved by fetoscopic temporary tracheal occlusion.

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9.  The independent effects of hyperventilation, tolazoline, and dopamine on infants with persistent pulmonary hypertension.

Authors:  W H Drummond; G A Gregory; M A Heymann; R A Phibbs
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10.  Congenital diaphragmatic hernia: arterial structural changes and persistent pulmonary hypertension after surgical repair.

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8.  Perinatal factors associated with poor neurocognitive outcome in early school age congenital diaphragmatic hernia survivors.

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9.  Evaluation of congenital diaphragmatic hernia in a tertiary health center of a developing country: management and survival.

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10.  Shifting from laparotomy to thoracoscopic repair of congenital diaphragmatic hernia in neonates: early experience.

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